“Die Zulassung der neuen Formulierung von Rebif in Europa ist ein weiterer wichtiger Erfolg unserer Anstrengungen Patienten mit MS immer bessere therapeutisch Optionen zu bieten,” sagte Roberto Gradnik, der bei Lusqo Tplque yde Lrxuye udspmmndt ont. “Wdb grjekl mgw, Rhvrsvzsh vp week Kwlkzc xisfn wnwffpzapuc Xsojscthkvbcuzb ddzkrlrx sm zuvtjj.”
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